Bachelor's degree in nursing, allied medical professions or other health care field required or equivalent combination of education and experience required; Current State of Ohio nursing license or other relevant board or interim permit required in appropriate field; clinical research certification ...
Successful candidates would be expected to participate in the clinical, educational, and research activities of the Center for Cognitive and Memory Disorders, a multidisciplinary group with behavioral neurologists, neuropsychiatrists, research scientists, neuropsychologists, psychometrists, social w...
Serves as Manager, CCRM Clinical Research Operations in the College of Medicine (COM) Center for Clinical Research Management (CCRM); participates in execution of activities in the CCRM Clinical Research Operations Office in collaboration with Directors-Clinical Research Operations; oversees multipl...
Desired skills include: Clinical research Dosage ranges Indications Ethical Research Principles & Practices Side effects Keen attention to detail Medical terminology Microsoft Office proficiency Licensing or Certifications for Clinical Research Nurse and Physician Assi...
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Department of Neurosurgery; assists with assessing patient records to identify patients who ...
The Clinical Consultant Research works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice (GCP) guidelines and federal regulations. Clinical Research Coordinator Certification (or equivalent approved Clinic...
Provides assistance in support of clinical research studies being conducted in the Department of Emergency Medicine; participates in the recruitment of study participants; collects and provides relevant data to be used in assessing eligibility of patients for participation in protocols; assists with...
Bachelor's degree in nursing, allied medical professions or other health care field required or equivalent combination of education and experience required; Current State of Ohio nursing license or other relevant board or interim permit required in appropriate field; clinical research certification ...
Serves as Manager, CCRM Clinical Research Operations in the College of Medicine (COM) Center for Clinical Research Management (CCRM); participates in execution of activities in the CCRM Clinical Research Operations Office in collaboration with Directors-Clinical Research Operations; oversees multipl...
Duties will include supervision of clinical research coordinators, health coaches, and undergraduate research students, as well as data and budget management, oversight of IRB submissions and safety reporting, and preparing/submitting conference abstracts and research manuscripts. The clinical resea...
As part of patient facing duties, the Senior Clinical Research Assistant participates in coordinating and performing clinical research activities for assigned studies, including therapeutic studies involving SOC or FDA approved drugs/devices, in accordance with approved protocols; assists with asses...
We are seeking a full-time Clinical Research Coordinator to join Principal Investigator Dr Sarah O’Brien’s research laboratory. Dr O’Brien’s research focuses on the intersections between women’s health and hematology and seeks to improve recognition of bleeding disorders in women. Performing researc...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
Serves as the contact for physicians, nurses and other ancillary hospital staff to assure that all research and related clinical needs are achieved. Maintains accurate awareness of all clinical projects within the research center. YEARS OF EXPERIENCE: 3-5 years critical care experience required with...
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the ; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, inter...
Clinical Research Coordinator III (RN) performs tasks independently, consistently and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities resulting in high quality work. KPA 1 Protocol Comprehension and Implementation: Coordination o...
Clinical Research Senior Coordinator serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the oversees, implements & coordinates conduct of daily activities of research studies; recruits, interviews and promotes study to...
The Clinical Research Coordinator II is responsible for managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. Conducts clinical studies as outlined in the study prot...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Senior Clinical Research Associate positions open for a Biotechnology client. The ideal CRA will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating p...
Summary:The Clinical Consultant Research works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice (GCP) guidelines and federal regulations. Clinical Research Coordinator Certification (or equivalent approve...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...